Development of a strain for efficient degradation of polychlorinated biphenyls by patchwork assembly of degradation pathways

Rhodococcus jostii RHA1 accumulates chlorobenzoates (CBA) during the degradation of polychlorinated biphenyls (PCBs). CBA degradation is considered one of the rate-limiting steps in the complete degradation of PCBs. To reduce the accumulation of CBAs, the upper pathway enzyme genes for PCB degradation of RHA1 were introduced into a CBA-degrading bacterium, Burkholderia sp. NK8. The resulting recombinant strain exhibited no biphenyl 2,3-dioxygenase (BphA) activity encoded by bphAaAbAcAd genes, which encode the large and small subunits of the terminal oxygenase component and the ferredoxin and reductase subunits responsible for electron transfer from NADH to the large subunit. The remaining enzyme genes involved in the transformation of biphenyl to benzoate, bphB2C1D1, which encode dehydrogenase, ring-cleavage dioxygenase and hydrolase, conferred activities to NK8. To obtain the BphA activity of RHA1 in NK8, sets of BphA genes were constructed by combining the bphAaAbAcAd genes of RHA1 and bphA3A4 of Pseudomonas pseudoalcaligenes KF707, encoding the ferredoxin and reductase subunits. Hybrid derivatives of BphA containing the KF707 bphA3 conferred BphA activity to NK8, and a derivative containing the RHA1 bphAaAb and KF707 bphA3A4 genes exhibited the highest BphA activity. A plasmid containing the RHA1 bphAaAb and KF707 bphA3A4 genes plus the RHA1 bphB2C1D1 genes was constructed and introduced into NK8. The resulting recombinant strain efficiently degraded 2-, 3- and 4-chlorobiphenyls with an apparent reduction in CBA accumulation in comparison to the recombinant mutant strain, which had an insertion in the cbeA gene to inactivate CBA dioxygenase.     

Electron pulse radiolysis determination of hydroxyl radical rate constants with Suwannee River fulvic acid and other dissolved organic matter isolates

Pulse radiolysis experiments were conducted on dissolved organic matter (DOM) samples isolated as hydrophobic and hydrophilic acids and neutrals from different sources (i.e., stream, lake, wastewater treatment plant). Absolute bimolecular reaction rate constants for the reaction of hydroxyl radicals (*OH) with DOM (k*(OH), DOM) were determined. k*(OH, DOM) values are expressed as moles of carbon. Based on direct measurement of transient DOM radicals (DOM*) and competition kinetic techniques, both using pulse radiolysis, the k*(OH, DOM) value for a standard fulvic acid from the Suwannee River purchased from the International Humic Substances Society was (1.60 +/- 0.24) x 10(8) M(-1) s(-1). Both pulse radiolysis methods yielded comparable k*(OH, DOM) values. The k*(OH, DOM) values for the seven DOM isolates from different sources ranged from 1.39 x 10(8) M(-1) s(-1) to 4.53 x 10(8) M(-1) s(-1), and averaged 2.23 x 108 M(-1) s(-1) (equivalent to 1.9 x 10(4) (mgC/L)(-1) s(-1)). These values represent the first direct measurements of k*(OH, DOM,) and they compare well with literature values obtained via competition kinetic techniques during ozone or ultraviolet irradiation experiments. More polar, lower-molecular-weight DOM isolates from wastewater have higher k*(OH, DOM) values. In addition, the formation (microsecond time scale) and decay (millisecond time scale) of DOM* transients were observed for the first time. DOM* from hydrophobic acids exhibited broader absorbance spectra than transphilic acids, while wastewater DOM isolates had narrower DOM* spectra more skewed toward shorter wavelengths than did DOM* spectra for hydrophobic acids.     

Microporous activated carbons from used coffee grounds for application to electric double‐layer capacitors

Electrochemical double‐layer capacitors (EDLCs) are devices that store enormous amounts of charge electrostatically when a potential is applied between electrodes of very high surface area (typically made of porous carbon) and an electrolyte. Wider commercialization of this technology has been held back by the lack of ultralow‐cost electrode materials. We demonstrate that used coffee grounds can be processed to form low‐cost electrodes. The surface and electrochemical characteristics of microporous activated carbons from used coffee grounds (CGCs) were measured. First, optimal times and temperatures for carbonization and activation were identified on the basis of Brunauer–Emmett–Teller (BET) surface area, pore volume, and pore size distribution. Second, CGCs were used as polarized electrodes in EDLCs, whose capacitances were evaluated using cyclic voltammetry. The results show that carbonization for 1 h at 600 °C with a heating rate of 300 °C/h, followed by CO₂ activation for 2 h at 1000 °C, affords the highest BET surface area (1867 m²/g) compared to other works. The produced CGCs have many micropores of less than 2 nm across, which contribute to the formation of an electric double layer. Capacitors made using these CGCs show the highest capacitance (103 F/g) in 0.8 M (C₂H₅)₄NBF₄/PC as an organic electrolyte, which is much higher than the ∼80 F/g typically used in organic‐electrolyte‐based commercial EDLCs, suggesting that coffee grounds are a useful electrode material. © 2014 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Estimation of daily intake of phenols in hospital meal samples

Daily intakes of 12 phenols which are possible endocrine disruptors were estimated in hospital meals from 2000 to 2001. 4-Nonylphenol (4-NP (mix)) and bisphenol A (BPA) were detected at levels of 5.0 to 19.4 ng/g and 0.2 to 1.1 ng/g, respectively. 4-tert-Butylphenol, 4-n-pentylphenol, 4 -tert-pentylphenol, 4-n-hexylphenol, 4-n-heptylphenol and 4-tert-octylphenol were detected at levels of 0.1 to 2.4 microg/g. The daily intakes of 4-NP (mix) and BPA were 5.8 microg/day and 0.42 microg/day, respectively. The daily intakes of other phenols were less than 1 microg/day.     

Influence of quadrature‐axis reactance of large turbine generator on operation

Two‐pole large generators are extensively used in power utilities. Growing demand for electric power in recent years has led to substantial increases in the capacity of generators. In line with this trend, our company has manufactured two‐pole turbine generators in the 900,000‐kVA to 1,200,000‐kVA classes. As the capacity of generators becomes larger, equivalent circuits are increasingly expected to improve their precision in estimating operation characteristics. The Park model has been widely used as an equivalent circuit model. The Park model with quadrature axis transient reactance $x_{q}^{\prime}$ is claimed to be useful for accurately estimating the load rejection characteristics of turbine generators. However, it is difficult to measure $x_{q}^{\prime}$, few studies based on measured data have appeared. As one of the few examples, we have conducted a measured data on a 500,000‐kVA‐class generator. Recently, the authors obtained test data on $x_{q}^{\prime}$ of a 900,000‐kVA‐class generator. In this study, based on these data, we studied the effect of $x_{q}^{\prime}$ using the finite element method and a transient analysis program (EMTP‐ATP). © 2011 Wiley Periodicals, Inc. Electr Eng Jpn, 177(3): 17–27, 2011; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.21099     

具有缺陷和应力限值的预应力钢支撑柱屈曲性能

通过预应力支撑加固的钢柱,一般增加了轴向抗压强度。过去,十分强调获得更高的临界屈曲荷载,然而,后屈曲性能是结构安全性和功能的重要保证。对具有几何缺陷和与可能的材料失效相关的应力极限的支撑柱的屈曲性能进行检验。考虑有几何缺陷支撑柱的屈曲性能,采用Rayleigh-Ritz方法对几何非线性模型公式化,并通过有限元方法进行验证。研究显示：对于承受最高临界荷载的预应力状态,系统对有几何缺陷的柱更为敏感。对某一给定形状结构,实际的最大荷载似乎随着预应力的增加而增加。研究建议：最佳的预应力取值应该大于基于传统方法的线性分析的结果。     

Chiral sensing system based on the formation of diastereomeric metal complex on a homocysteine monolayer using field effect transistor

A self-assembled monolayer (SAM) of l-homocysteine (l-Hcy) formed on the surface of a gold-deposited gate of a field effect transistor (FET) was used to differentiate between enantiomers of amino acids, for which the formation of diastereomeric metal complexes is fundamental for chiral discrimination. Here, we focus our attention on the dependence of the FET response on the analyte amino acids, the central metal ions involved in complex formation, and the solution pH. Using the l-Hcy SAM-modified gate with added Cu(II), notable negative FET responses were enantioselectively observed for the l-enantiomers of alanine (Ala), phenylalanine, and tryptophan, whereas differences in the FET responses between enantiomers were negligible for asparagine and aspartic acid. Regarding the enantioselectivity for Ala, the addition of Cu(II) was demonstrated to show higher selectivity as compared to other metal ions such as Co(II) and Ni(II). Moreover, for the addition of l-Ala and Cu(II), a particularly strong negative FET response was observed at pH 5.5.     

Unit commitment scheduling by Lagrange relaxation method taking into account transmission losses

Since the application of the Lagrange relaxation method to the unit commitment scheduling by Muckstadt in 1979, many papers using this method have been published. The greatest advantage of applying the Lagrange relaxation method for the unit commitment problem is that it can relax (ignore) each generator's output dependency caused by the demand–supply balance constraint so that a unit commitment of each generator is determined independently by dynamic programming. However, when we introduce the transmission loss into the demand–supply balance constraint, we cannot decompose the problem into the partial problems in which each generator's unit commitment is determined independently and have to take some measures to obtain an optimal schedule by the Lagrange relaxation method directly. In this paper, we present an algorithm for the unit commitment schedule using the Lagrange relaxation method for the case of taking into account transmission losses. © 2005 Wiley Periodicals, Inc. Electr Eng Jpn, 152(4): 27–33, 2005; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20119     

Large area ZnO films optimized for graded band-gap Cu(InGa)Se2-based thin-film mini-modules

In this study, two deposition methods (i.e. MOCVD and sputtering methods) to prepare n-type ZnO window layers for CIGS-based thin-film solar cells are discussed. In order to make ZnO : Al transparent conductive oxide (TCO) films prepared by DC magnetron sputtering comparable to ZnO : B TCO prepared by MOCVD, a new ZnO sputtering process is proposed by introducing a multilayer structure. Using these films, CIGS thin-film solar cells with efficiencies of greater than 14% have been fabricated with an active area of 3.2 cm². This structure was adapted to fabricate CIGS thin-film mini-modules with efficiencies around 11% having aperture area of 50 cm².     

Mechanochemical Effects on the Formation and Properties of Various Nickel Phosphates

Mixtures of ammonium dihydrogen phosphate and basic nickel carbonate with P/Ni molar ratios of 2/3, 1/1, and 2/1 were ground in a planetary mill. The thermal behavior of the milled samples was investigated by differential thermal analysis, x-ray diffraction, and Fourier transform infrared spectroscopy. In addition, the samples were characterized by ultraviolet-visible reflectance spectroscopy, particle size distribution, scanning electron microscopy, and nitrogen adsorption measurements. As a result of mechanochemical effects, the targeted nickel phosphates were formed at lower temperatures, had a more vivid color, and consisted of more regularly shaped particles.